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The contribution of NOD2 gene mutations to the risk and site of disease in inflammatory bowel disease.
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CARD15/NOD2 mutational analysis and genotype-phenotype correlation in 612 patients with inflammatory bowel disease.
Am J Hum Genet. 2002 Apr;70(4):845-57. doi: 10.1086/339432. Epub 2002 Mar 1.
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Association between insertion mutation in NOD2 gene and Crohn's disease in German and British populations.
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A frameshift mutation in NOD2 associated with susceptibility to Crohn's disease.
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Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn's disease.
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A polymorphism in the gene for microsomal epoxide hydrolase is associated with pre-eclampsia.
J Med Genet. 2001 Apr;38(4):234-7. doi: 10.1136/jmg.38.4.234.
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High-activity microsomal epoxide hydrolase genotypes and the risk of oral, pharynx, and larynx cancers.
Cancer Res. 2000 Feb 1;60(3):534-6.
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A multiplex-PCR/RFLP procedure for simultaneous CYP2E1, mEH and GSTM1 genotyping.
Cancer Lett. 1999 Aug 23;143(1):51-6. doi: 10.1016/s0304-3835(99)00192-5.
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Genetic polymorphisms of human N-acetyltransferase, cytochrome P450, glutathione-S-transferase, and epoxide hydrolase enzymes: relevance to xenobiotic metabolism and toxicity.
Crit Rev Toxicol. 1999 Jan;29(1):59-124. doi: 10.1080/10408449991349186.
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A genomewide analysis provides evidence for novel linkages in inflammatory bowel disease in a large European cohort.
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